ChemicalBook >> CAS DataBase List >>3-Bromoquinoline

3-Bromoquinoline

CAS No.
5332-24-1
Chemical Name:
3-Bromoquinoline
Synonyms
Bromoquinoline;Quinoline, 3-bromo-;NSC 3995;CETH-016;3-BromoquinoL;3-BROMOQUINOLINE;3-BROMOQUINLIINE;3-bromo-quinolin;3-Bromoquuinoline;1-3-Bromoquinoline
CBNumber:
CB4220082
Molecular Formula:
C9H6BrN
Molecular Weight:
208.05
MDL Number:
MFCD00006767
MOL File:
5332-24-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 02:26:29
Product description Number Pack Size Price
3-Bromoquinoline 98% 124133 25g $131
3-Bromoquinoline 98% 124133 100g $262.5
3-Bromoquinoline >98.0%(GC)(T) B1013 25g $86
3-Bromoquinoline Asreported 262039 5g $275
3-Bromoquinoline Asreported 262039 10g $362
More product size

3-Bromoquinoline Properties

Melting point 13-15 °C (lit.)
Boiling point 274-276 °C (lit.)
Density 1.533 g/mL at 25 °C (lit.)
vapor pressure 0.196Pa at 25℃
refractive index n20/D 1.664(lit.)
Flash point >230 °F
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka 2.69(at 25℃)
form Liquid
color Clear colorless to yellow
Water Solubility 103mg/L at 25℃
BRN 112939
InChI 1S/C9H6BrN/c10-8-5-7-3-1-2-4-9(7)11-6-8/h1-6H
InChIKey ZGIKWINFUGEQEO-UHFFFAOYSA-N
SMILES Brc1cnc2ccccc2c1
LogP 3.03
CAS DataBase Reference 5332-24-1(CAS DataBase Reference)
FDA UNII ZRP57JF73Z
NIST Chemistry Reference Quinoline, 3-bromo-(5332-24-1)
EPA Substance Registry System Quinoline, 3-bromo- (5332-24-1)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
PPE Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
RIDADR  UN2810
WGK Germany  3
TSCA  TSCA listed
HS Code  29334900
Storage Class 10 - Combustible liquids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
REACH Registrations Inactive
NFPA 704
1
2 0

3-Bromoquinoline price More Price(77)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 124133 3-Bromoquinoline 98% 5332-24-1 25g $131 2026-04-30 Buy
Sigma-Aldrich 124133 3-Bromoquinoline 98% 5332-24-1 100g $262.5 2026-04-30 Buy
TCI Chemical B1013 3-Bromoquinoline >98.0%(GC)(T) 5332-24-1 25g $86 2026-04-30 Buy
Usbiological 262039 3-Bromoquinoline Asreported 5332-24-1 5g $275 2026-06-03 Buy
Usbiological 262039 3-Bromoquinoline Asreported 5332-24-1 10g $362 2026-06-03 Buy
Product number Packaging Price Buy
124133 25g $131 Buy
124133 100g $262.5 Buy
B1013 25g $86 Buy
262039 5g $275 Buy
262039 10g $362 Buy

3-Bromoquinoline Chemical Properties,Uses,Production

Bromoquinoline

There are seven position isomers with the main properties are as follows:

Name
Melting point(℃)
Boiling point(℃)
Solubility
2-bromoquinoline
48~49
It is soluble in diethyl ether, chloroform and benzene
3-bromoquinoline
12~15
274~276, 95(66.66Pa)
4-bromoquinoline
29~30
270(decomposition)
Easily soluble in dilute acid
5-bromoquinoline
52 (needle crystal)
280
6-bromoquinoline
24
278
7-bromoquinoline
52 (needle crystal)
290
8-bromoquinoline
80
165~166
(2399.79Pa)

Application and synthesis method

3-Bromoquinoline can have action with mixed acid to generate 3-bromo-5-nitroquinoline, followed by heating with potassium permanganate to be oxidized to 5-bromo-2, 3-pyridine dicarboxylic acid.
6-bromo-quinoline can be heated together nitric acid to generate 6-bromo-8-nitro-quinoline, followed by reaction with potassium permanganate to be oxidized into 2, 3-pyridinedicarboxylic acid.
2-bromo-quinoline can be manufactured through the reaction between 2-hydroxyquinoline and phosphorus pentabromide
3-bromo-quinoline can be obtained through heating the quinoline perbromide at 180 ° C.
4-bromoquinoline can be obtained through either the heating reaction between 4-hydroxyquinoline and phosphorus pentabromide or by the diazotization reaction of 4-aminoquinoline.
5-bromo-quinoline can be obtained from the heating reaction between m-bromo aniline, glycerol, m-bromonitrobenzene and concentrated sulfuric acid, or through the diazotization reaction of 5-amino-quinoline.
6-bromo-quinoline can be obtained through the heating reaction between p-bromoaniline, glycerol, concentrated sulfuric acid and p-bromo-nitrobenzene.
7-bromoquinoline can be obtained through the diazotization of 7-aminoquinoline.
8-bromo-quinoline can be obtained through the heating of o-bromo aniline, glycerol, concentrated sulfuric acid and o-bromo-nitrobenzene in the heating system.
Purposes: as organic synthesis reagents.

Uses

For pharmaceuticals
Medicine, pesticide intermediates

Chemical Properties

colorless to light yellow liquid

Uses

3-Bromoquinoline undergoes bromine-magnesium exchange reaction with lithium tributylmagnesate in toluene at -10°C, which is quenched by various electrophiles to yield functionalized quinolines.

Synthesis Reference(s)

The Journal of Organic Chemistry, 27, p. 1318, 1962 DOI: 10.1021/jo01051a047

General Description

3-Bromoquinoline undergoes bromine-magnesium exchange reaction with lithium tributylmagnesate in toluene at -10°C, which is quenched by various electrophiles to yield functionalized quinolines.

Flammability and Explosibility

Not classified

References

[1] Patent: US3956301, 1976, A
[2] Patent: US5266700, 1993, A

Global( 429)Suppliers
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View Lastest Price from 3-Bromoquinoline manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
3-Bromoquinoline pictures 2026-06-04 3-Bromoquinoline
5332-24-1
$11.00-119.00 25g 0.98 25kg Shanghai UCHEM Inc.
3-Bromoquinoline  pictures 2025-11-18 3-Bromoquinoline
5332-24-1
$1.10 1g 99.00% 100 Tons Dideu Industries Group Limited
3-Bromoquinoline pictures 2025-04-04 3-Bromoquinoline
5332-24-1
1KG 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
3-bromo-quinolin 3-BROMOQUINLIINE 3-BROMOQUINOLINE Quinoline, 3-bromo- 3-Bromoquinoline98%Or99% 3-Bromoquinoline 98 % 3-Bromoquinoline ,98% [HPLC 98%] 3-BroMoquinoline, 98% 25GR CETH-016 NSC 3995 Quinolin-3-yl broMide 3 - broMine generation of quinoline 3-BroMoquinoline, 98.0%(GC&T 3 - broMine quinoline 3-BromoquinoL 3-Bromoquinoline > 3-Bromoquinoline ISO 9001:2015 REACH 1-3-Bromoquinoline 3-Bromoquuinoline 3-Bromoquinoline - [B4614] Bromoquinoline 5332-24-1 1532-71-5 C9H6NBr Haloquinolines Quinolines Building Blocks Halogenated Heterocycles Heterocyclic Building Blocks Aromatics Compounds Haloquinolines Aromatics Quinoline&Isoquinoline Quinoline Derivertives Building Blocks Halogenated Heterocycles Heterocyclic Building Blocks QuinolinesHeterocyclic Building Blocks Quinolines, Quinazolines and derivatives Halides Heterocycles blocks Bromides Quinolines